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AQA GCSE Chemistry
Revision NotesAddition Polymerisation
Addition Polymerisation
Definition of Addition Polymerisation
Addition polymerisation is a type of reaction where monomers containing carbon 6carbon double bonds (C=C) join together to form a polymer chain. In this process, the double bonds break and the monomers link up without the loss of any small molecules. This is different from condensation polymerisation, where small molecules like water are released.
Monomers and Polymers
The monomers involved in addition polymerisation are usually alkenes, which have at least one C=C double bond. During polymerisation, these monomers open up their double bonds and join together to form long chains called polymers. The repeating unit in the polymer is derived from the original monomer.
For example, ethene (C2H4) is an alkene monomer. When many ethene molecules join together, they form poly(ethene), commonly known as polythene or polyethylene.
The repeating unit in poly(ethene) is 6CH2 6CH2 6, which comes from the ethene monomer after the double bond breaks and the monomers link up.
For instance, the polymerisation of ethene can be represented as:
Polymerisation Process
The key step in addition polymerisation is the breaking of the C=C double bond in the alkene monomer. This double bond consists of one sigma ( 3 4) bond and one pi ( 1 2) bond. The 1 2 bond is weaker and breaks during the reaction, allowing the monomers to join by forming new single (sigma) bonds.
As the double bond breaks, each monomer forms single bonds with neighbouring monomers, creating a long chain. This process repeats many times, causing the polymer chain to grow.
The general mechanism involves the following:
- Breaking the C=C double bond in each monomer
- Forming single bonds between carbon atoms of adjacent monomers
- Continuing the chain growth until many monomers are linked
For example, during the polymerisation of propene (C3H6), the double bond breaks and the monomers join to form poly(propene), with repeating units derived from the original monomer.
Example: The polymerisation of ethene involves breaking the C=C double bond in each ethene molecule, then linking the molecules together to form a long chain of poly(ethene).
Uses and Properties of Addition Polymers
Addition polymers are widely used as plastics in everyday life. Common examples include:
- Poly(ethene) (polythene) 6 used in plastic bags, bottles, and containers
- Poly(propene) (polypropylene) 6 used in packaging, ropes, and carpets
- Poly(chloroethene) (PVC) 6 used in pipes, window frames, and clothing
These polymers are generally inert and unreactive due to their strong carbon 6carbon single bonds and lack of reactive functional groups. This makes them durable but also means they do not biodegrade easily, leading to environmental concerns.
Worked Example
Example: Write the repeating unit for the polymer formed from the monomer propene (C3H6).
Worked Example
Example: Explain why no small molecules are released during addition polymerisation.
Worked Example
Example: Poly(chloroethene) (PVC) is made from the monomer chloroethene (vinyl chloride), which has the formula CH2=CHCl. Write the repeating unit of poly(chloroethene).
- Remember that addition polymerisation involves only alkenes with C=C bonds.
- Think of the polymer as a long chain made by "opening" the double bonds and linking monomers end to end.
- No small molecules are lost in addition polymerisation, unlike condensation polymerisation.
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